Dikoglu, E. Et Al. 2013. Homozygosity for a Novel Truncating Mutation Confirms TBX15 Deficiency as the Cause of Cousin Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.161, no.12 , 3161-3165.

Dikoglu, E., ŞİMŞEK KİPER, P. Ö., ÜTİNE, G. E., Campos-Xavier, B., BODUROĞLU, O. K., Bonafe, L., ... Superti-Furga, A.(2013). Homozygosity for a Novel Truncating Mutation Confirms TBX15 Deficiency as the Cause of Cousin Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.161, no.12, 3161-3165.

Dikoglu, Esra Et Al. "Homozygosity for a Novel Truncating Mutation Confirms TBX15 Deficiency as the Cause of Cousin Syndrome," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.161, no.12, 3161-3165, 2013

Dikoglu, Esra Et Al. "Homozygosity for a Novel Truncating Mutation Confirms TBX15 Deficiency as the Cause of Cousin Syndrome." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.161, no.12, pp.3161-3165, 2013

Dikoglu, E. Et Al. (2013) . "Homozygosity for a Novel Truncating Mutation Confirms TBX15 Deficiency as the Cause of Cousin Syndrome." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.161, no.12, pp.3161-3165.

@article{article, author={Esra Dikoglu Et Al. }, title={Homozygosity for a Novel Truncating Mutation Confirms TBX15 Deficiency as the Cause of Cousin Syndrome}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2013, pages={3161-3165} }